TRANSLATIONAL CONTROL BY CYTOPLASMIC POLYADENYLATION OF C-MOS MESSENGER-RNA IS NECESSARY FOR OOCYTE MATURATION IN THE MOUSE

The c-mos proto-oncogene product is a key element in the cascade of ev ents leading to meiotic maturation of vertebrate oocytes, We have inve stigated the role of cytoplasmic polyadenylation in the translational control of mouse c-mos mRNA and its contribution to meiosis, Using an RNase protection assay we show that optimal cytoplasmic polyadenylatio n of c-mos mRNA requires three cis elements in the 3' UTR: the polyade nylation hexanucleotide AAUAAA and two U-rich cytoplasmic polyadenylat ion elements (CPEs) located 4 and 51 nucleotides upstream of the hexan ucleotide. When fused to CAT coding sequences, the wild-type 3' UTR of c-mos mRNA, but not a 3' UTR containing mutations in both CPEs, confe rs translational recruitment during maturation, This recruitment coinc ides with maximum polyadenylation. To assess whether c-mos mRNA polyad enylation is necessary for maturation of mouse oocytes, we have ablate d endogenous c-mos mRNA by injecting an antisense oligonucleotide, whi ch results in a failure to progress to meiosis II after emission of th e first polar body, Such antisense oligonucleotide-injected oocytes co uld be efficiently rescued by co-injection of a c-mos mRNA carrying a wild-type 3' UTR, However, co-injection of a c-mos mRNA lacking functi onal CPEs substantially lowered the rescue activity, These results dem onstrate that translational control of c-mos mRNA by cytoplasmic polya denylation is necessary for normal development.